First-order rate constants for the hydrolysis of polyuridylic acid in
the absence and presence of various metal ions and their chelates have
been determined under neutral and slightly acidic conditions. The hyd
rolysis has been shown to proceed by cleavage of non-terminal bonds ra
ther han by stepwise release of monomeric nucleotides. Only the hydrol
ysis of the 3',5'-phosphodiester bonds is accelerated by metal ions, n
ot their isomerization to 2',5'-bonds. The catalytically active specie
s has been shown to be the monohydroxo form of the metal aquo ion. The
rate accelerations are parallel, but up to 20 times greater than thos
e obtained with uridylyl(2',5') uridine. The mechanism of the metal-io
n action is discussed.